Alignments for a candidate for aacS in Sphingomonas koreensis DSMZ 15582

GapMind for catabolism of small carbon sources

Alignments for a candidate for aacS in Sphingomonas koreensis DSMZ 15582

Align Acetoacetate--CoA ligase (EC 6.2.1.16) (characterized)
to candidate Ga0059261_0835 Ga0059261_0835 Acyl-CoA synthetases (AMP-forming)/AMP-acid ligases II

Query= reanno::acidovorax_3H11:Ac3H11_3009
         (578 letters)



>FitnessBrowser__Korea:Ga0059261_0835
          Length = 582

 Score =  243 bits (619), Expect = 2e-68
 Identities = 174/548 (31%), Positives = 270/548 (49%), Gaps = 47/548 (8%)

Query: 46  EALVSVHQGRRYTYAQLQTEAHRLASALLGMGLTPGDRVGIWSHNNAEWVLMQLATAQVG 105
           + + ++H+  R ++        RLA+ L  MG+  GDRV +   N  EW ++  A   +G
Sbjct: 66  DRIFTIHEDERVSFEANFRAVARLATQLREMGVGKGDRVALAMRNLPEWPVVFFAAVSIG 125

Query: 106 LVLVNINPAYRTAEVEYALNKVGCKLLVSMARFKTSDYLGMLRELAPEWQGQQPGHLQAA 165
            +LV +N  + + E++Y L   G     S+  F   +    L +  P             
Sbjct: 126 AILVPLNAWWTSGELDYGLRDSG-----SVVLFTDGERYDRLADALPG------------ 168

Query: 166 KLPQLKTVVWIDDEAGQGADEPGLLRFTELIAR-GNAADPRLAQVAA--GLQATDPINIQ 222
            LP LK +V       +G    G+ +  +LI + G+ A+   A + A   L   D   I 
Sbjct: 169 -LPDLKHIVV---SRARGPLGEGVRQLEDLIGKPGDWAELPDAPLPAEPSLVPDDDATIF 224

Query: 223 FTSGTTGFPKGATLTHRNILNNGFFIGEC----------MKLTPADRLCIPV-PLYHCFG 271
           +TSGTTG PKGA  THRN++ N    G C          M   P  R+ + V PL+H   
Sbjct: 225 YTSGTTGHPKGALGTHRNLITNILSSGYCGARPYLRRGEMPPDPTPRVGLMVIPLFHVTA 284

Query: 272 MVLGNLACFTHGATIVYPNDGFDPLTVLQTVQDERCTGLHGVPTMFIAELDHPRFAEFNL 331
                +     G T ++    +D    ++ +Q E+     GVPT+    L+HP  A+++L
Sbjct: 285 CSASLMGAVFAGHTTIFMRK-WDVEQAMEIIQREKVNLTGGVPTIAWQLLEHPARAKYDL 343

Query: 332 STLRTGIMAGSPCPTEVMKRVVEQMNLREITIAYGMTETSPVSCQSSTDTPLSKRVSTVG 391
           S+L      G+P   E++KR+  +         +GMTET     Q S +  L+ R ++ G
Sbjct: 344 SSLEMIAYGGAPSAPELVKRIYTEFGALPGN-GWGMTETMATVTQHSAEDYLN-RPTSAG 401

Query: 392 QVQPHLEVKIVDPDTGAVVPIGQRGEFCTKGYSVMHGYWGDEAKTREAIDEGGWMHTGDL 451
              P  E+KI+D +    +PIG+ GE   KG  ++ GYW    +T E+  +G W+ TGDL
Sbjct: 402 PPVPVAELKIMDAEGEHELPIGEVGELWAKGPMIVKGYWNKPEETAESFRDG-WVRTGDL 460

Query: 452 ATMDAEGYVNIVGRIKDMVIRGGENIYPREIEEFLYRHPQVQDVQVVGVPDQKYGEELCA 511
           A +D EG++ IV R KD++IRGGENIY  E+E+ LY HP V D  ++G+P +  GEE  A
Sbjct: 461 ARVDEEGFLFIVDRAKDIIIRGGENIYSSEVEDVLYAHPAVTDAALIGIPHRTLGEEPVA 520

Query: 512 WIIAKPGTQPTEDDIRAFCKGQIAHYKVPRYIRFV-TSFPMTVTGKIQKFKIRDEMKDQL 570
            +   PG Q +E +++ + + ++A +KVP  IRF   + P    GKI K       KD  
Sbjct: 521 VVHLAPGKQASEAELQQWVRDRLAAFKVPVAIRFTRDTLPRNANGKILK-------KDLK 573

Query: 571 GLEEQKTA 578
           GL  ++ A
Sbjct: 574 GLFAEEAA 581


Lambda     K      H
   0.320    0.136    0.412 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 808
Number of extensions: 46
Number of successful extensions: 5
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 1
Number of HSP's successfully gapped: 1
Length of query: 578
Length of database: 582
Length adjustment: 36
Effective length of query: 542
Effective length of database: 546
Effective search space:   295932
Effective search space used:   295932
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 53 (25.0 bits)

This GapMind analysis is from Apr 09 2024. The underlying query database was built on Sep 17 2021.

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Protein sequences (fasta format)
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About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see:

the paper from 2019 on GapMind for amino acid biosynthesis
the 2024 update on GapMind for amino acid biosynthesis
the paper from 2022 on GapMind for carbon sources
the source code
instructions for running GapMind on your computer

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory

GapMind for catabolism of small carbon sources